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Balamapimod

  Cat. No.:  DC10994  
Chemical Structure
863029-99-6
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More than 5000 active chemicals with high quality for research!
Field of application
Balamapimod (MKI-833) is an orally active, reversible Ras/Raf/MEK inhibitor developed for antineoplastic potential..
Cas No.: 863029-99-6
Chemical Name: 4-[[3-Chloro-4-[(1-methyl-1H-imidazol-2-yl)thio]phenyl]amino]-6-methoxy-7-[4-(1-pyrrolidinyl)-1-piperidinyl]-3-quinolinecarbonitrile
Synonyms: MKI-833;MKI833
SMILES: N1C2C(=CC(OC)=C(N3CCC(N4CCCC4)CC3)C=2)C(NC2=CC=C(SC3N(C)C=CN=3)C(Cl)=C2)=C(C#N)C=1
Formula: C30H32ClN7Os
M.Wt: 574.144
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: Balamapimod (MKI-833) is an orally active, reversible Ras/Raf/MEK inhibitor developed for antineoplastic potential.
Cat. No. Product name Field of application
DC42418 ML786 dihydrochloride ML786 dihydrochloride potent and orally bioavailable Raf, with IC50s of 2.1, 4.2, and 2.5 nM for V600EΔB-Raf, wt B-Raf, and C-Raf, respectively. ML786 dihydrochloride also inhibits Abl-1, DDR2, EPHA2, KDR, and RET (IC50=<0.5, 7.0, 11, 6.2, 0.8 nM). ML786 dihydrochloride can be used for the research of cancers.
DC8777 CEP-32496 hydrochloride CEP-32496 Hcl is a highly potent inhibitor of BRAF(V600E/WT) and c-Raf with Kd of 14 nM/36 nM and 39 nM, also potent to Abl-1, c-Kit, Ret, PDGFRβ and VEGFR2, respectively; insignificant affinity for MEK-1, MEK-2, ERK-1 and ERK-2.
DC10994 Balamapimod Balamapimod (MKI-833) is an orally active, reversible Ras/Raf/MEK inhibitor developed for antineoplastic potential..
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